Author details

Full Name

Rui Chen

Affiliation

ORCID

Career Start Year

1997

Papers

219

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36821256	Experimental demonstration of real-time optical DFT-S DMT signal transmission for a blue-LED-based UWOC system using spatial diversity reception.		2023
37633553	Helicase-independent function of RIG-I against murine gammaherpesvirus 68 via blocking the nuclear translocation of viral proteins.		2023
37773233	Insights into the protective immune response by immunization with full-length recombinant TprK protein: cellular and humoral responses.		2023
37770468	Author Correction: Spatial organization of the mouse retina at single cell resolution by MERFISH.		2023
37347187	Longitudinal Variations in the Gene of Treponema pallidum in an Amoy Strain-Infected Rabbit Model.		2023
37287420	Emotional and behavioral problems change the development of cerebellar gray matter volume, thickness, and surface area from childhood to adolescence: A longitudinal cohort study.		2023
36842237	Biomimetic dendritic polymeric microspheres induce enhanced T cell activation and expansion for adoptive tumor immunotherapy.		2023
36515158	From multi-omics data to the cancer druggable gene discovery: a novel machine learning-based approach.		2023
35348597	Assessing Variant Causality and Severity Using Retinal Pigment Epithelial Cells Derived from Stargardt Disease Patients.	Transl Vis Sci Technol	2022
35771864	Integration of multidimensional splicing data and GWAS summary statistics for risk gene discovery.	PLoS Genet	2022
35459094	A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization.	BMC Bioinformatics	2022
35898448	Baseline Testosterone Predicts Body Composition and Metabolic Response to Testosterone Therapy.	Frontiers in Endocrinology	2022
36140798	Exome Sequencing Identified Molecular Determinants of Retinal Dystrophies in Nine Consanguineous Pakistani Families.	Genes	2022
35368022	Spata7 is required for maintenance of the retinal connecting cilium.	Scientific Reports	2022
36270621	Deciphering the developmental order and microstructural patterns of early white matter pathways in a diffusion MRI based fetal brain atlas.	NeuroImage	2022
35486108	Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily.	Genet Med	2022
36323073	Activation of the cGAS-STING pathway combined with CRISPR-Cas9 gene editing triggering long-term immunotherapy.	Biomaterials	2022
35353811	Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease.	PLoS Genet	2022
35665818	One-Year Mean A1c ofâ¿¿>â¿¿7% is Associated with Poor Bone Microarchitecture and Strength in Men with Type 2 Diabetes Mellitus.	Calcified Tissue International	2022
35038348	Comparative ligandomics implicates secretogranin III as a disease-restricted angiogenic factor in laser-induced choroidal neovascularization.		2022
34855657	Use of Diterpene Ginkgolides Meglumine Injection to Regulate Plasma Levels of PAI-1 and t-PA in Patients With Acute Atherosclerotic Cerebral Infarction.	Neurologist	2022
34728399	The Relationship Between APOE Gene Polymorphism and In-stent Restenosis After Stenting at the Beginning of the Vertebral Artery.	World Neurosurgery	2022
34726245	Cwc27, associated with retinal degeneration, functions as a splicing factor in vivo.	Human Molecular Genetics	2022
35205424	Leveraging Gene-Level Prediction as Informative Covariate in Hypothesis Weighting Improves Power for Rare Variant Association Studies.	Genes	2022
34897697	Clinical presentation, treatment, and genetic and histopathological analysis of juvenile cataracts and secondary glaucoma in a rhesus macaque (Macaca mulatta).	J Med Primatol	2022
35181798	Diagnostic accuracy of vesical imaging-reporting and data system (VI-RADS) for the detection of muscle-invasive bladder cancer: a meta-analysis.	Abdominal Radiology	2022
35165951	Retinal organoids derived from rhesus macaque iPSCs undergo accelerated differentiation compared to human stem cells.	Cell Proliferation	2022
35012639	Artificial intelligence framework identifies candidate targets for drug repurposing in Alzheimer's disease.	Alzheimers Res Ther	2022
35100262	The Ets protein Pointed P1 represses Asense expression in type II neuroblasts by activating Tailless.	PLoS Genetics	2022
35116328	Systematic analysis of the long noncoding RNA (lncRNA)-miRNA-mRNA competing endogenous RNA network to identify prognostic biomarkers and the potential regulatory axis in glioblastoma multiforme.	Translational Cancer Research	2021
34297801	Single-Cell Transcriptomics Identifies a Unique Entity and Signature Markers of Transit-Amplifying Cells in Human Corneal Limbus.	Investigative Ophthalmology and Visual Science	2021
34290089	Nuclear NAD homeostasis governed by NMNAT1 prevents apoptosis of acute myeloid leukemia stem cells.	Science advances	2021
33907365	Noncoding mutation in <i>RPGRIP1</i> contributes to inherited retinal degenerations.	Mol Vis	2021
33537757	In Men With Obesity, T2DM Is Associated With Poor Trabecular Microarchitecture and Bone Strength and Low Bone Turnover.	Journal of Clinical Endocrinology and Metabolism	2021
34232885	Stratified Test Accurately Identifies Differentially Expressed Genes Under Batch Effects in Single-Cell Data.	IEEE/ACM Trans Comput Biol Bioinform	2021
33737949	Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases.	Front Genet	2021
34104971	Transcript isoforms of Reep6 have distinct functions in the retina.	Human Molecular Genetics	2021
33718653	Testosterone therapy and bone quality in men with diabetes and hypogonadism: Study design and protocol.	Contemporary Clinical Trials Communications	2021
33556050	Homeodomain protein Six4 prevents the generation of supernumerary Drosophila type II neuroblasts and premature differentiation of intermediate neural progenitors.	PLoS Genetics	2021
34087851	Effects of chromosomal abnormalities on pregnancy outcomes in female undergoing artificial insemination with donor's sperm.	Medicine (United States)	2021
33599254	Subtype-GAN: a deep learning approach for integrative cancer subtyping of multi-omics data.	Bioinformatics	2021
33436941	The molecular mechanisms of the long noncoding RNA SBF2-AS1 in regulating the proliferation of oesophageal squamous cell carcinoma.	Scientific Reports	2021
32884132	A novel statistical method for interpreting the pathogenicity of rare variants.	Genetics in Medicine	2021
34733980	Preliminary study of the use of E6/E7mRNA detection in screening and triage management of HR-HPV infection during pregnancy.	Annals of Translational Medicine (discontinued)	2021
35027909	Hemoglobin A1c Threshold for Reduction in Bone Turnover in Men With Type 2 Diabetes Mellitus.	Frontiers in Endocrinology	2021
32499757	Aromatase Inhibitors Plus Weight Loss Improves the Hormonal Profile of Obese Hypogonadal Men Without Causing Major Side Effects.	Frontiers in Endocrinology	2020
32265282	Mapping the <i>cis</i>-regulatory architecture of the human retina reveals noncoding genetic variation in disease.	Proc Natl Acad Sci U S A	2020
32367481	Role of Chromatin Remodeling Genes and TETs in the Development of Human Midbrain Dopaminergic Neurons.	Stem Cell Reviews and Reports	2020
31786788	Single-Cell Capture, RNA-seq, and Transcriptome Analysis from the Neural Retina.	Methods in Molecular Biology	2020
32356724	A big-data approach to understanding metabolic rate and response to obesity in laboratory mice.	eLife	2020